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3-Phenylprop-2-Enal → 4-Chloro-3,3-dimethyl-6-phenylhex-5-en-2-one

HRID 981796
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인쇄 미리보기

반응식

HRID 981796 반응식
[CH:1](=O)[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH:11]([C:14]([CH3:16])=[O:15])([CH3:13])[CH3:12].[ClH:17].C(=O)([O-])[O-].[Na+].[Na+]>>[C:4]1([CH:3]=[CH:2][CH:1]([Cl:17])[C:11]([CH3:13])([CH3:12])[C:14](=[O:15])[CH3:16])[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 3073-Phenylprop-2-EnalHCID 313Hydrochloric AcidHCID 10340Sodium CarbonateHCID 112513-Methyl-2-butanone

생성물 1

HCID 541173564-Chloro-3,3-dimethyl-6-phenylhex-5-en-2-one

실험 절차

20 g (0.15 mol) of cinnamaldehyde and 25.8 g (0.3 mol) of methyl isopropyl ketone are initially introduced, and dry hydrogen chloride is passed in at 10° C. until saturation. The mixture is stirred for 12 hours at 20°-25° C. and poured onto water, and the resulting mixture is neutralized by means of sodium carbonate. The neutralized mixture is extracted with methylene chloride and dried, and the methylene chloride is distilled off. 25.7 g (72.4% of theory) are obtained of 1-phenyl-3-chloro-4,4-dimethyl-1-hexen-5-one which has a melting point of 71° C.

후처리

  1. customis passed in at 10° C. until saturation
  2. additionpoured onto water
  3. extractionThe neutralized mixture is extracted with methylene chloride
  4. customdried
  5. distillationthe methylene chloride is distilled off

출처 및 근거

ORD 기록
ord-4560a2f37cc8474885424e9f5afa7a65
출처 데이터셋
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04992577

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